US4435368A - Hydrometallurgical process for selective dissolution of mixtures of oxy compounds - Google Patents
Hydrometallurgical process for selective dissolution of mixtures of oxy compounds Download PDFInfo
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- US4435368A US4435368A US06/086,791 US8679179A US4435368A US 4435368 A US4435368 A US 4435368A US 8679179 A US8679179 A US 8679179A US 4435368 A US4435368 A US 4435368A
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- 239000000203 mixture Substances 0.000 title claims abstract description 81
- 238000004090 dissolution Methods 0.000 title claims abstract description 30
- 238000009854 hydrometallurgy Methods 0.000 title description 2
- 239000011133 lead Substances 0.000 claims abstract description 42
- 239000000460 chlorine Substances 0.000 claims abstract description 33
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 29
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 29
- 239000008346 aqueous phase Substances 0.000 claims abstract description 20
- 238000000034 method Methods 0.000 claims abstract description 20
- 239000010949 copper Substances 0.000 claims abstract description 17
- 229910017052 cobalt Inorganic materials 0.000 claims abstract description 16
- 239000010941 cobalt Substances 0.000 claims abstract description 16
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims abstract description 16
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 12
- 150000001875 compounds Chemical class 0.000 claims abstract description 12
- 229910052802 copper Inorganic materials 0.000 claims abstract description 12
- 239000007900 aqueous suspension Substances 0.000 claims abstract description 7
- 239000007864 aqueous solution Substances 0.000 claims abstract 2
- 229910000480 nickel oxide Inorganic materials 0.000 claims description 3
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 claims description 3
- 150000002816 nickel compounds Chemical class 0.000 claims 4
- 229910000008 nickel(II) carbonate Inorganic materials 0.000 claims 1
- ZULUUIKRFGGGTL-UHFFFAOYSA-L nickel(ii) carbonate Chemical compound [Ni+2].[O-]C([O-])=O ZULUUIKRFGGGTL-UHFFFAOYSA-L 0.000 claims 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract description 70
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 43
- 229910052759 nickel Inorganic materials 0.000 abstract description 31
- 229910052751 metal Inorganic materials 0.000 abstract description 19
- 239000002184 metal Substances 0.000 abstract description 19
- 239000000725 suspension Substances 0.000 abstract description 19
- 229910052742 iron Inorganic materials 0.000 abstract description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract description 11
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract description 8
- 239000011707 mineral Substances 0.000 abstract description 8
- 239000011701 zinc Substances 0.000 abstract description 7
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract description 6
- 229910052725 zinc Inorganic materials 0.000 abstract description 6
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 abstract description 5
- 238000009835 boiling Methods 0.000 abstract description 2
- 239000000428 dust Substances 0.000 abstract description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 abstract description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 abstract 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract 1
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 abstract 1
- 229910052710 silicon Inorganic materials 0.000 abstract 1
- 239000010703 silicon Substances 0.000 abstract 1
- 238000005406 washing Methods 0.000 description 33
- 239000000243 solution Substances 0.000 description 30
- 239000000047 product Substances 0.000 description 29
- 239000011575 calcium Substances 0.000 description 26
- 239000003643 water by type Substances 0.000 description 25
- 239000011777 magnesium Substances 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- 238000006243 chemical reaction Methods 0.000 description 18
- 239000011572 manganese Substances 0.000 description 16
- JBQYATWDVHIOAR-UHFFFAOYSA-N tellanylidenegermanium Chemical compound [Te]=[Ge] JBQYATWDVHIOAR-UHFFFAOYSA-N 0.000 description 16
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 14
- 229910052791 calcium Inorganic materials 0.000 description 14
- 239000012452 mother liquor Substances 0.000 description 11
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 10
- 239000005864 Sulphur Substances 0.000 description 10
- 229910052749 magnesium Inorganic materials 0.000 description 10
- 229910052748 manganese Inorganic materials 0.000 description 9
- 229910021653 sulphate ion Inorganic materials 0.000 description 9
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 8
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 7
- 150000002739 metals Chemical class 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- 239000011651 chromium Substances 0.000 description 6
- -1 ferrous metals Chemical class 0.000 description 6
- 239000007790 solid phase Substances 0.000 description 6
- 239000004411 aluminium Substances 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 239000007791 liquid phase Substances 0.000 description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 3
- 241000694440 Colpidium aqueous Species 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 229910052797 bismuth Inorganic materials 0.000 description 3
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- 229910052804 chromium Inorganic materials 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229910052793 cadmium Inorganic materials 0.000 description 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 2
- QHFQAJHNDKBRBO-UHFFFAOYSA-L calcium chloride hexahydrate Chemical compound O.O.O.O.O.O.[Cl-].[Cl-].[Ca+2] QHFQAJHNDKBRBO-UHFFFAOYSA-L 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229910000464 lead oxide Inorganic materials 0.000 description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 description 2
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 239000002893 slag Substances 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 229910000010 zinc carbonate Inorganic materials 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- 229910018404 Al2 O3 Inorganic materials 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- QVYYOKWPCQYKEY-UHFFFAOYSA-N [Fe].[Co] Chemical compound [Fe].[Co] QVYYOKWPCQYKEY-UHFFFAOYSA-N 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- ONIOAEVPMYCHKX-UHFFFAOYSA-N carbonic acid;zinc Chemical compound [Zn].OC(O)=O ONIOAEVPMYCHKX-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 1
- PXHVJJICTQNCMI-YPZZEJLDSA-N nickel-57 Chemical compound [57Ni] PXHVJJICTQNCMI-YPZZEJLDSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229910052705 radium Inorganic materials 0.000 description 1
- HCWPIIXVSYCSAN-UHFFFAOYSA-N radium atom Chemical compound [Ra] HCWPIIXVSYCSAN-UHFFFAOYSA-N 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B7/00—Working up raw materials other than ores, e.g. scrap, to produce non-ferrous metals and compounds thereof; Methods of a general interest or applied to the winning of more than two metals
- C22B7/02—Working-up flue dust
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B13/00—Obtaining lead
- C22B13/04—Obtaining lead by wet processes
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B15/00—Obtaining copper
- C22B15/0063—Hydrometallurgy
- C22B15/0065—Leaching or slurrying
- C22B15/0067—Leaching or slurrying with acids or salts thereof
- C22B15/0069—Leaching or slurrying with acids or salts thereof containing halogen
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B19/00—Obtaining zinc or zinc oxide
- C22B19/20—Obtaining zinc otherwise than by distilling
- C22B19/22—Obtaining zinc otherwise than by distilling with leaching with acids
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B23/00—Obtaining nickel or cobalt
- C22B23/04—Obtaining nickel or cobalt by wet processes
- C22B23/0407—Leaching processes
- C22B23/0415—Leaching processes with acids or salt solutions except ammonium salts solutions
- C22B23/0423—Halogenated acids or salts thereof
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
- C22B3/04—Extraction of metal compounds from ores or concentrates by wet processes by leaching
- C22B3/06—Extraction of metal compounds from ores or concentrates by wet processes by leaching in inorganic acid solutions, e.g. with acids generated in situ; in inorganic salt solutions other than ammonium salt solutions
- C22B3/10—Hydrochloric acid, other halogenated acids or salts thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Definitions
- the present invention relates to a hydrometallurgical process for the selective dissolution of mixtures of metallic oxy compounds; it relates particularly to the selective putting into solution of certain non-ferrous metals present in these mixtures.
- the metallurgist In the course of the putting into operation of processes by which pure metal is obtained from mineral, the metallurgist often meets mixtures of metallic oxy compounds. These mixtures can be met at any stage of the extraction of the metal, from the mineral, which can be a mixed oxide, up to the residues from the refining of the metals.
- an aim of the invention is to provide a process of selective dissolution of nickel oxide which allows it to be separated from oxides of cobalt, lead and copper.
- Another aim of the invention is to provide a process of selective dissolution of zinc oxide which allows it to be separated from oxides of copper and lead.
- Another aim of the invention is to provide a process of selective dissolution of copper oxide which allows it to be separated from lead oxide.
- This process consists essentially in putting into suspension in an aqueous phase the mixture of oxides to be treated and then subjecting this suspension to the action of chlorine.
- oxygenated compounds as used herein is intended to include a large number of compounds including oxides, hydroxides, carbonates, basic carbonates, and even certain sulphates and silicates.
- the chlorine necessary for the operation of this process is introduced in any convenient manner; it can thus be synthesised in situ by chemical or electrochemical means or introduced into the solution in the form of gaseous chlorine.
- the selectivity of the dissolution depends greatly on the pH and it is important to keep the pH beyond certain values which vary according to the oxide which it is desired to preferentially dissolve; in general, the pH should not be below the value of 1-2 and more often 3-4; this why it can be necessary to provide systems to keep a minimum pH. This is particularly important whilst the mixture contains much sulphur in its elemental form or as sulphide; the oxidation of sulphur by chlorine indeed causes a significant liberation of acidity.
- FIGURE of the drawing is a diagramatic flowsheet of the process according to the invention.
- the mixture of oxygenated compounds to be treated arrives at 1 in an apparatus A where it is suspended in a solution which is introduced at 2.
- the suspension which leaves at 3 from A enters a reactor B where it is subjected to the action of gaseous chlorine which is introduced at 5.
- the solution obtained after the reaction is removed from B at 6 and introduced at 7 into a decanting vessel D where the larger particles are separated from the solution and removed in the form of a suspension at 9.
- the thus clarified solution is led into a filtration apparatus C where the solid and liquid phases are then separated; the solid phase is removed at 11 whilst the liquid phase is drawn off at 12 and is passed to another type of apparatus (not shown) where it is subjected to further treatments to produce metal salts or pure metals.
- the solid phase which leaves at 11 from C is led at 13 into an apparatus A' in which it is subjected to suspension in an aqueous phase which enters at 14; this aqueous phase can be water, or a solution derived from another stage of the dissolution process if it is desired to operate an apparatus consisting of more than 2 stages.
- the stage of decantation can sometimes be omitted, in which case the solution which leaves at 6 from B is directly passed into the vessel C at 10.
- the resultant suspension kept under constant agitation, was then brought to the working temperature. Injection of chlorine into the reactor was then commenced and continued during the duration of the reaction. At regular intervals, samples were taken in order that the course of the reaction should be followed.
- the reaction mixture was filtered and the mother liquor recovered; the residual cake was then washed with water and the washing water covered. The mother liquor, the washing water and the residual cake were analysed. The cake could then be subjected to a new dissolution in chlorine. Then, the co-efficient of selectivity K was calculated according to the formula: ##EQU1## e.g., if Nickel is the regarded metal and if Iron is the impurity: ##EQU2##
- a trial for a continuous period of five days was carried out on a micropilot scale according to the scheme represented in FIG. 1.
- the lixiviation of the oxide was carried out in two cascade reactors of about 2 liters, the first being fed with the initial oxide previously suspended in the filtrate obtained from the outlet of the second reactor which, itself, is fed by a suspension in water of the residue leaving the second reactor.
- the temperatures and durations of lixiviation were identical in each reactor and respectively equal to 95° C. and 12 hours.
- the rate of feed of oxide was 25 g per hour and that of the incoming water was 170 ml per hour.
- the charge of chlorine was equal to twice the stoichiometric quantity with respect to nickel, namely 41 g per hour.
- the mineral treated was composed essentially of clay (SiO 2 +Al 2 O 3 +MgO), of carbonates (CaCO 3 -MgCO 3 ), of iron oxide (limonite), of lead oxide and of smithsonite (ZnCO 3 ).
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Metallurgy (AREA)
- Environmental & Geological Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Inorganic Chemistry (AREA)
- Geochemistry & Mineralogy (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Removal Of Specific Substances (AREA)
- Catalysts (AREA)
- Treatment Of Liquids With Adsorbents In General (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
The invention provides a process for the selective dissolution of oxygenated compounds containing at least one non-ferrous metal selected from the group consisting of nickel, zinc, and copper, present in a mixture of oxygenated compounds containing said at least one non-ferrous metal and at least one element selected from the group consisting of lead, cobalt, iron, manganese, and silicon, and comprises suspending the mixture of the oxygenated metallic compounds in an aqueous phase which, preferably, contains chloride and alkaline earth metal ions; treating the resulting aqueous suspension, maintained at a pH exceeding about 1, with chlorine, preferably at a temperature ranging from about 60 DEG C. to the boiling point of the suspension, to selectively solubilize the said at least one non-ferrous metal while the said at least one element remains in an essentially insoluble residue; and separating the aqueous solution containing the dissolved said at least one non-ferrous metal from the insoluble residue. The starting mixture of the oxygenated compounds is exemplified by the product resulting from the roasting of a nickel matte, a basic carbonate of nickel, a mineral oxide of zinc, and the dust of a blast furnace.
Description
This is a continuation of application Ser. No. 950,446, filed Oct. 11, 1978, which is a continuation of 904,306, filed May 9, 1978, now abandoned, which is also a continuation of 765,813, filed Feb. 4, 1977, now abandoned.
The present invention relates to a hydrometallurgical process for the selective dissolution of mixtures of metallic oxy compounds; it relates particularly to the selective putting into solution of certain non-ferrous metals present in these mixtures.
In the course of the putting into operation of processes by which pure metal is obtained from mineral, the metallurgist often meets mixtures of metallic oxy compounds. These mixtures can be met at any stage of the extraction of the metal, from the mineral, which can be a mixed oxide, up to the residues from the refining of the metals. One may cite as examples of such mixtures, the products of roasting of pyrites, the products of roasting of nickel mattes and the basic carbonates of nickel (B.N.C.) which are derived from a first reduction of the mineral following ammoniacal lixiviation.
In order to continue the process of extraction of the metal or metals, it is necessary to separate one from the other and, in particular to separate iron which is very often present in minerals of non-ferrous metals and which is then found in variable proportions in the first stages of the purification of these metals.
To carry out this separation, one proceeds, in general, to put into solution the metals to be recovered; this dissolution is most often done by means of hydrochloric or sulphuric acid; however, these dissolutions are not selective and appreciable amounts of iron are found in the final solutions.
This is why it is an aim of the invention to provide a process for the selective dissolution of oxides of non-ferrous metals which permits their separation from iron, manganese and silica. PG,5
More particularly, an aim of the invention is to provide a process of selective dissolution of nickel oxide which allows it to be separated from oxides of cobalt, lead and copper.
Another aim of the invention is to provide a process of selective dissolution of zinc oxide which allows it to be separated from oxides of copper and lead.
Another aim of the invention is to provide a process of selective dissolution of copper oxide which allows it to be separated from lead oxide.
According to the invention, these aims and others which will become apparent later are obtained by means of a process described below.
This process consists essentially in putting into suspension in an aqueous phase the mixture of oxides to be treated and then subjecting this suspension to the action of chlorine.
The term "oxygenated compounds" as used herein is intended to include a large number of compounds including oxides, hydroxides, carbonates, basic carbonates, and even certain sulphates and silicates.
The chlorine necessary for the operation of this process is introduced in any convenient manner; it can thus be synthesised in situ by chemical or electrochemical means or introduced into the solution in the form of gaseous chlorine.
Although it is possible to carry out the process at elevated temperatures, it is more convenient to perform the dissolution at a temperature below that of the boiling point of water and preferably between 60° and 100° C.
The selectivity of the dissolution depends greatly on the pH and it is important to keep the pH beyond certain values which vary according to the oxide which it is desired to preferentially dissolve; in general, the pH should not be below the value of 1-2 and more often 3-4; this why it can be necessary to provide systems to keep a minimum pH. This is particularly important whilst the mixture contains much sulphur in its elemental form or as sulphide; the oxidation of sulphur by chlorine indeed causes a significant liberation of acidity.
It is also possible to vary the selectivity of the dissolution by varying the composition, the complexing agents such as the chloride ion and the pH of the aqueous phase which serves to suspend the mixture of oxygenated compounds.
Thus, strong concentrations of chloride ion bring about an easier solution of the metals which form the complexes with the chloride ion.
It may also be noted that the presence of calcium ions strongly lowers the concentration of sulphate ions and thus allows an easier dissolution of metals which have insoluble sulphates and particularly of lead; by contrast, the presence of sulphate ions prevents the dissolution of plumbous ions.
This process of dissolution is particularly noteworthy by reason of its selectivity. At first, only the zinc and the nickel are dissolved, then as the process is continued copper is dissolved, and then lead which only dissolves in aqueous phases which are rich both in chloride ions and in ions of alkaline earth metals (calcium, strontium, barium, radium). Neither iron, manganese, cobalt nor silica are dissolved appreciably.
It will be appreciated that such a selective dissolution process is advantageous; indeed, not only does it allow separation of nickel and cobalt, or of zinc, copper and lead, but it also allows the purification of iron, cobalt and manganese which remain insoluble in these conditions.
The invention will be further described with reference to a preferred embodiment indicated in the accompanying drawing, but this description is not limitative of the invention.
The single FIGURE of the drawing is a diagramatic flowsheet of the process according to the invention.
Referring to this FIGURE, the mixture of oxygenated compounds to be treated arrives at 1 in an apparatus A where it is suspended in a solution which is introduced at 2. The suspension which leaves at 3 from A enters a reactor B where it is subjected to the action of gaseous chlorine which is introduced at 5.
The solution obtained after the reaction is removed from B at 6 and introduced at 7 into a decanting vessel D where the larger particles are separated from the solution and removed in the form of a suspension at 9. The thus clarified solution is led into a filtration apparatus C where the solid and liquid phases are then separated; the solid phase is removed at 11 whilst the liquid phase is drawn off at 12 and is passed to another type of apparatus (not shown) where it is subjected to further treatments to produce metal salts or pure metals.
The solid phase which leaves at 11 from C is led at 13 into an apparatus A' in which it is subjected to suspension in an aqueous phase which enters at 14; this aqueous phase can be water, or a solution derived from another stage of the dissolution process if it is desired to operate an apparatus consisting of more than 2 stages. The suspension leaves at 15 from A' and enters at 16 a reactor B' in which it is mixed with the suspension which leaves at 9 from D and which enters at 18 into B'; the mixture of the two suspensions is then subjected to a bubbling of chlorine which is introduced into the vessel B' at 17.
The solution which leaves at 19 from B' is led at 20 into a filtration apparatus C' where the solid and liquid phases are separated; the liquid phase is recovered at 22 and returned at 2 into A, whilst the solid phase is removed at 21; the solid phase can be discarded, or subjected to a further dissolution in the case of a multistage installation.
The stage of decantation can sometimes be omitted, in which case the solution which leaves at 6 from B is directly passed into the vessel C at 10.
The following non-limitative examples are provided to further illustrate the invention and to enable the experts to determine the suitable operating conditions in each particular case.
In the tables below, the abbreviation "n.d." means "not determined".
In a reactor equipped with a cooling coil, an agitator, a thermometer and a pipe for injection of chlorine, there was poured the desired amount of water or of a solution of sodium chloride or calcium chloride, and then the mixture of oxygenated compounds was added either in one batch or little by little.
The resultant suspension, kept under constant agitation, was then brought to the working temperature. Injection of chlorine into the reactor was then commenced and continued during the duration of the reaction. At regular intervals, samples were taken in order that the course of the reaction should be followed.
At the end of the reaction, the reaction mixture was filtered and the mother liquor recovered; the residual cake was then washed with water and the washing water covered. The mother liquor, the washing water and the residual cake were analysed. The cake could then be subjected to a new dissolution in chlorine. Then, the co-efficient of selectivity K was calculated according to the formula: ##EQU1## e.g., if Nickel is the regarded metal and if Iron is the impurity: ##EQU2##
______________________________________
Mixture to be treated
1 kg of wet B.N.C. con-
taining 16.89% by weight
of nickel
Aqueous phase for the
500 ml water
suspension
Amount of chlorine injected
40 g per hour
Duration of the reaction
7 hours
Working temperature
75° C.
______________________________________
(a) Change in pH and amount of nickel in solution as a function of time
______________________________________
Duration of the
Amount of Ni.sup.++ in
pH of reaction mixture
reaction (hours)
the solutions obtained
at 75° C.
______________________________________
0 0.040 7.5
1/2 6.2 6.1
1 15.8 5.8
2 36.0 5.4
3 54.4 4.8
4 73.0 4.3
5 84.2 4.0
6 87.0 3.7
______________________________________
(b) Results of the dissolution.
The results of the analysis of the cake, the mother-liquors and the washing waters are given in the following table together with the composition of the starting mixture:
__________________________________________________________________________
COMPOSITION
of the of the
initial
of the
of the
cake
K with
product
mother-
washing
(fully
respect to
(dry)
liquor
waters
dry)
iron (mother-
(%) (g/l) (g/l) (%) liquor)
__________________________________________________________________________
Nickel (Ni)
47.00
97 52 50 590
Cobalt (Co)
0.65 3.4.10.sup.-3
0.6.10.sup.-3
4.40
1.3
Iron (Fe) 0.20 0.7.10.sup.-3
≦0.2.10.sup.-3
0.95
Manganese (Mn)
0.05 0.5.10.sup.-3
≦0.1.10.sup.-3
0.31
2.9
Zinc (Zn) 0.08 0.18 32.10.sup.-3
nd 640
Copper (Cu)
0.07 0.018 2.3.10.sup.-3
nd 72
Lead (Pb) ≦0.001
nd nd nd
Sulphate (SO.sub.4.sup.--)
4.95 17.8 4.3 2.60
Total Sulphur (S)
2.41 5.9 1.5 0.96
Carbon dioxide (CO.sub.2)
6.99 nd nd nd
Ammonia (NH.sub.3)
0.51 ≦20.10.sup.-3
≦20.10.sup.-3
nd
Chromium (Cr)
≦0.002
nd nd nd
Aluminium (Al)
≦0.005
nd nd nd
Bismuth (Bi)
≦0.005
nd nd nd
Tin (Sn) ≦0.005
nd nd nd
Sodium (Na)
<0.01
nd nd nd
Calcium (Ca)
nd nd nd nd
__________________________________________________________________________
Final pH 3.7
Volume of mother-liquor recovered
760 ml
Volume of washing water recovered
1240 ml
Dry weight of residual cake 50 g
Yield of the dissolution of the nickel
85%
__________________________________________________________________________
______________________________________
Mixture to be treated
1000 g of B.N.C.
containing 16.89% of
nickel
Aqueous phase for the
500 ml of 1 M sodium
suspension chloride
Amount of chlorine 40 g per hour
injected
Duration of the reaction
5 hours
Working temperature
75° C.
______________________________________
The results of the analysis of the cake, the mother-liquor and the washing water are given in the following table together with the composition of the (fully dry) starting mixture:
__________________________________________________________________________
COMPOSITION
of the
dried
of the
of the K with
initial
mother-
washing
of the
respect to
product
liquors
waters
cake iron (mother-
(%) (g/l)
(g/l) (%) liquors)
__________________________________________________________________________
Nickel (Ni)
47.00
105 36.5 51 110
Cobalt (Co)
0.65 0.13 0.004 3.90 1
Iron (Fe) 0.70 0.004
0.002 0.71 --
Manganese (Mn)
0.05 ≦0.0001
≦0.0001
0.23 <1
Zinc (Zn) 0.08 0.150
0.049 0.034
108
Copper (Cu)
0.07 0.025
0.0046
0.23 18
Lead (Pb) ≦0.001
0.001
≦0.0001
0.0005
50≦
Sulphate (SO.sub.4.sup.--)
4.95 20.0 1.95
Total sulphur (S)
2.41 6.6 1.30
Carbon dioxide (CO.sub.2)
6.99 nd
Ammonia (NH.sub.3)
0.51 nd
Chromium (Cr)
≦0.002
nd
Aluminium (Al)
≦0.005
nd
Bismuth (Bi)
≦0.005
nd
Tin (Sn) ≦0.005
nd
Sodium (Na)
<0.01
15
__________________________________________________________________________
Volume of mother-liquor 850 ml
Volume of washing water recovered
1200 ml
Dry weight of residual cake 68 g
Yield of the dissolution of the nickel
79.3%
__________________________________________________________________________
______________________________________
Mixture to be treated
1000 g of B.N.C.
containing 16.89%
nickel
Aqueous phase for the
500 ml of 1.3 M calcium
suspension chloride solution
Amount of chlorine injected
1.3 M
Duration of the reaction
6 hours
Working temperature
75° C.
______________________________________
The results of the analysis of the cake, the mother-liquor and the washing water are given in the following table, together with the composition of the starting mixture:
__________________________________________________________________________
COMPOSITION
of the
dried
of the
of the K with
initial
mother-
washing
of the
respect to
product
liquors
waters
cake iron (mother-
(%) (g/l)
(g/l) (%) liquor)
__________________________________________________________________________
Nickel (Ni)
47.00
91 48 38.8 390
Cobalt (Co)
0.65 0.01 0.005 2.9 3
Iron (Fe) 0.70 0.001
0.0007
0.47
Manganese (Mn)
0.05 0.002
0.0008
1.56 8
Zinc (Zn) 0.08 0.120
0.066 0.018
300
Copper (Cu)
0.07 0.044
0.015 0.15 125
Lead (Pb) ≦0.0001
0.026
0.008 0.0005
≦5000
Sulphate (SO.sub.4.sup.--)
4.95 1.9 2.2 18.23
Total sulphur (S)
2.41 nd
Carbon dioxide (CO.sub.2)
6.99 nd
Ammonia (NH.sub.3)
0.51 nd
Chromium (Cr)
≦0.002
nd
Aluminium (Al)
≦0.005
nd
Bismuth (Bi)
≦0.005
nd
Tin (Sn) ≦0.01
nd
Calcium (Ca) 13.8
__________________________________________________________________________
Volume of mother-liquors recovered
820 ml
Volume of washing waters recovered
1060 ml
Dry weight of residual cake 94.5 g
Yield of the dissolution of the nickel
77.2%
__________________________________________________________________________
______________________________________
Mixture to be treated
300 g of residue containing
80% water derived from a first
attack on B.N.C.
Aqueous phase for the
300 ml water
suspension
Amount of chlorine injected
40 g per liter
Duration of the reaction
5 hours
Working temperature
75° C.
______________________________________
The results of the analysis of the cake, the mother-liquors and the washing waters are given in the following table together with the composition of the starting mixture:
______________________________________
COMPOSITION
of the
dried of the of the
initial mother- washing
of the
product liquors waters cake
(%) (g/l) (g/l) (%)
______________________________________
Nickel (Ni) 45 65.80 22.10 45.5
Cobalt (Co) 2.63 0.003 0.03 9.95
Iron (Fe) 0.67 0.0001 0.0002 1.90
Manganese (Mn)
0.24 0.004 0.0002 0.63
Zinc (Zn) 0.040 0.110 0.037 0.025
Copper (Cu) 0.27 0.170 0.046 0.31
Lead (Pb) nd ≦0.0003
0.0003 ≦0.010
Sulphate (SO.sub.4.sup.--)
nd 5.50 1.80 1.14
Total sulphur (S)
nd 1.80 0.62 0.40
______________________________________
Volume of mother-liquors recovered
450 ml
Volume of washing waters recovered
430 ml
Dry weight of residual cake
22 g
Yield of the dissolution of the nickel
68.5%
Final pH 3.3
______________________________________
______________________________________
Mixture to be treated
134 g of a residue of
B.N.C. after two
successive attacks
Aqueous phase for the
180 ml water
suspension
Amount of chlorine injected
40 g per hour
Duration of the reaction
5 hours
Working temperature 75° C.
______________________________________
The results of the analysis of the cake, the mother-liquors and the washing waters are given in the following table together with the composition of the starting mixture:
______________________________________
COMPOSITION
of the
dried of the of the
initial mother- washing
of the
product liquors waters cake
(%) (g/l) (g/l) (%)
______________________________________
Nickel (Ni) 51 2.5 8.3 43
Cobalt (Co) 6.3 0.27 0.0007 11.30
Iron (Fe) 1.1 0.0009 0.0005 2.30
Manganese (Mn)
0.40 0.0002 0.0002 0.70
Zinc (Zn) 0.06 0.065 0.022 0.04
Copper (Cu) 0.38 0.20 0.059 0.34
Lead (Pb) nd 0.0002 0.0002 0.18
Sulphate (SO.sub.4.sup.--)
nd 1.20 0.58 1.13
Total sulphur (S)
nd 0.46 0.20 nd
______________________________________
Volume of mother-liquor recovered
175 ml
Volume of washing water recovered
220 ml
Dry weight of residual cake
10.5 g
Yield of the dissolution of the nickel
57%
Final pH 2.2
______________________________________
______________________________________
Mixture to be treated
125 g of an oxide derived
from moderate roasting of
a matte at about
700°-800° C.
Aqueous phase for the
1 liter of water
suspension
Duration of the introduction
6 hours
of the oxide
Amount of chlorine injected
37 g per hour
Duration of the addition of
6 hours
chlorine
Working temperature
95° C.
______________________________________
The reaction was allowed to continue for one hour after the end of the addition of chlorine.
The results of the analysis of the cake, the mother-liquors and the washing waters are given in the following table together with the composition of the starting mixture:
______________________________________
COMPOSITION
of the dried
of the mother-liquors
initial product
and the washing waters
% %
______________________________________
Nickel (Ni) 72.23 42
Cobalt (Co) 1.75 0.002
Iron (Fe) 3.25 0.002
Sulphate (SO.sub.4.sup.--)
nd 9.7
Total sulphur (S)
2.70 nd
______________________________________
Volume of mother-liquors recovered
110 ml
Volume of washing waters recovered
Yield of the dissolution of the nickel
45.5%
Final pH 5.0 (95° C.)
______________________________________
______________________________________
Mixture to be treated
125 g of an oxide derived
from moderate roasting of
a matte at about
700°-800° C.
Aqueous phase for the
1 liter of water
suspension
Duration of the introduction
5 hours (6.25 g each
of the oxide quarter hour)
Amount of chlorine injected
19 g per hour
Duration of the addition of
12 hours
chlorine
______________________________________
The reaction was allowed to continue for 7 hours after the end of the addition of chlorine.
The results of the analysis of the cake, the mother-liquors and the washing waters are given in the following table together with the composition of the starting mixture:
______________________________________
COMPOSITION
of the
dried of the of
initial
mother-liquor
the K with
product
& the wash-
cake respect to
% % % iron cobalt
______________________________________
Nickel (Ni)
72.23 53.6 46 1227 658
Cobalt (Co)
1.75 ≦0.002
4.7
Iron (Fe) 3.25 ≦0.002
9
Sulphate (SO.sub.4.sup.--)
nd 10.8 nd
Total sulphur (S)
2.70 nd
______________________________________
Volume of mother-liquor recovered
and 1110 ml
Volume of washing water recovered
Dry weight of residual cake 36 g
Yield of the dissolution of the nickel
78%
Final pH 3.4
______________________________________
Trial of continuous dissolution of an oxide of nickel
A trial for a continuous period of five days was carried out on a micropilot scale according to the scheme represented in FIG. 1. As the drawing shows, the lixiviation of the oxide was carried out in two cascade reactors of about 2 liters, the first being fed with the initial oxide previously suspended in the filtrate obtained from the outlet of the second reactor which, itself, is fed by a suspension in water of the residue leaving the second reactor.
The temperatures and durations of lixiviation were identical in each reactor and respectively equal to 95° C. and 12 hours. The rate of feed of oxide was 25 g per hour and that of the incoming water was 170 ml per hour. The charge of chlorine was equal to twice the stoichiometric quantity with respect to nickel, namely 41 g per hour.
After continuous operation of about 100 hours, there were obtained a solution of nickel chloride and a residue.
The results of the analysis of the residue and of the lixiviation solution are shown in the following table together with the composition of the starting mixture:
______________________________________
COMPOSITION
of the dried
of the K with
initial lixiviation respect to
product solution of the co-
% g/l residue
iron balt
______________________________________
Nickel (Ni)
68.8 84 22 1830 220
Cobalt (Co)
1.8 0.010 5.3
Iron (Fe) 3.0 ≦0.003
10.3
Total Sulphur (S)
2.30 2.9 0.17
______________________________________
Yield of the dissolution of nickel
84%
pH of the lixiviation solution
4.3
______________________________________
Treatment of a zinc oxide mineral obtained from the slag heaps of a paper factory in France
The mineral treated was composed essentially of clay (SiO2 +Al2 O3 +MgO), of carbonates (CaCO3 -MgCO3), of iron oxide (limonite), of lead oxide and of smithsonite (ZnCO3).
______________________________________
Mixture to be treated 129.4 g
Aqueous phase for the suspension
1000 ml of water
Charge of chlorine 20 g per hour
Duration of the reaction
6 hours
Working temperature 85° C.
______________________________________
KINETICS OF THE ATTACK
Composition
of the fully
dry starting Composition of the solution after
product (g/l)
Element (%) 1 h 2 h 3 h 4 h 5 h 6 h
______________________________________
Zinc (Zn)
8.2 6.70 7.04 7.56 7.64 7.68 7.72
Lead (Pb)
4.5 0 0 0 0 0.1 0.1
Magnesium
2.5 2.18 3.02 3.16 3.16 3.16 3.16
(Mg)
Calcium 5.1 3.76 4.88 4.95 5.15 5.20 5.20
(Ca)
Iron (Fe)
6.25
pH 3.5 2.9 2.35 2.32 1.9 2.1
Chloride
nd 20.15 33.02
32.84
34.79
34.26
32.84
(Cl.sup.-)
______________________________________
__________________________________________________________________________
BALANCE SHEET OF THE ATTACK
Yield of
Composition
COMPOSITION the attack
of the fully
of the
of the
of the with res-
dry starting
starting
mother-
washing
of the
pect to the
product
solution
liquors
waters
residue
initial
Element (%) (g/l)
(g/l)
(g/l)
(%) product
__________________________________________________________________________
Zinc (Zn)
8.2 0 7.95 0.78 1.8 85.9
Lead (Pb)
4.5 0 0.12 0 6.3 2.5
Magnesium (mg)
2.5 0 3.2 0.32 0.08
98.4
Calcium (Ca)
5.1 0 5.1 0.55 0.22
97
Iron (Fe)
6.25 0 -- -- 8 --
__________________________________________________________________________
Volume of mother-liquor recovered
1050 ml
Volume of washing waters recovered
500 ml
Weight of residual cake 79.8 g
__________________________________________________________________________
______________________________________
Mixture to be treated
123 g of a mineral
obtained from the slag
heaps of a paper factory
in France
Aqueous phase for the suspension
1000 ml of a solution
containing 180.8 g of
magnesium chloride and
1786.7 g of calcium
chloride hexahydrate
Charge of chlorine 8.6 g per hour
Duration of the reaction
7 hours
Working temperature 85° C.
______________________________________
KINETICS OF THE ATTACK
Composition
of the fully
dry starting
Composition of the solution after
Ele- product (g/l)
ment (%) 1 h 2 h 3 h 4 h 5 h 6 h 7 h
______________________________________
Zinc 8.2 6.70 7.10 7.15 7.20 7.25 7.30 7.36
(Zn)
Lead 4.5 5.1 5.2 5.0 4.7 4.3 4.4 4.2
(Pb)
pH 3.2 2.8 2.8 2.8 3.3 3.1 3.1
______________________________________
__________________________________________________________________________
BALANCE SHEET OF THE ATTACK
Yield of
Composition
COMPOSITION the attack
of the fully
of the
of the
of the with res-
dry starting
starting
mother-
washing
of the
pect to the
product
solution
liquors
waters
residue
initial
Element (%) (g/l)
(g/l)
(g/l)
(%) product
__________________________________________________________________________
Zinc (Zn)
8.2 0 7.30 0.09 2.13
78.5
Lead (Pb)
4.5 0 4.35 0.23 1.25
78.8
Magnesium (Mg)
2.5 0.49
84.8
Calcium (Ca)
5.1 4.25
35.5
Iron (Fe)
6.25 0 6.65
__________________________________________________________________________
Volume of mother-liquor recovered
1010 ml
Volume of washing waters recovered
500 ml
Weight of residual cake 95.5 g
__________________________________________________________________________
Attack on the dusts from the smoke of the blast furnaces of Anzin
__________________________________________________________________________
Mixture to be treated 100 g of dusts from the smoke
Aqueous phase for the suspension
1000 ml of water
Charge of chlorine 8 g per hour
Duration of the reaction 51/2 hours
Working temperature 85° C.
__________________________________________________________________________
KINETICS OF THE ATTACK
Composition
of the fully
dry starting
Composition of the solution after
product
(g/l)
Element (%) 30 m
1 h 2 h 3 h 4 h 5 h 5.30 h
7 h
__________________________________________________________________________
Zinc (Zn)
10.08 1 1.4 4 6.1 6.9 7.2 7.7
Lead (Pb)
6.88 -- -- -- -- -- 0.37
0.45
Magnesium (Mg)
2.32 0.05
0.4 1 1.45
1.5 1.55
1.6
Calcium (Ca)
8.8 2.1 2.1 2.8 3.3 4.1 4.1 4.1
Iron (Fe)
27 <0.001
0.001
0.0015
0.002
0.009
0.076
0.056
pH 6.9 6.85
4.8 2.9 2.5 2.4 2.4
Chloride (Cl.sup.-)
4 5.7 12.8 17.8
20.6
22.2
22.3
__________________________________________________________________________
__________________________________________________________________________
BALANCE SHEET OF THE ATTACK
Yield of
Composition
COMPOSITION the attack
of the fully
of the
of the with res-
dry starting
mother-
washing
of the
pect to the
product
liquors
waters
residue
initial
Element (%) (g/l)
(g/l)
(%) product
__________________________________________________________________________
Zinc (Zn) 10.08 5.38 0.34 5.57
50.7
Lead (Pb) 6.88 0.31 0.008
6.93
4.5
Magnesium (Mg)
2.32 1.67 0.09 0.76
70.2
Calcium (Ca)
8.8 5.65 0.81 2.80
69.3
Iron (Fe) 27 0.015
0.002
22.43
Cadmium (Cd)
0.05
Manganese (Mn)
3.96
Silver (Ag)
88 ppm
Silica (SiO.sub.2)
3.68-3.76
Aluminium (Al.sub.2 O.sub.3)
0.91
__________________________________________________________________________
__________________________________________________________________________
Mixture to be treated 100 g of dust from blast
furnaces
Aqueous phase for the suspension
1000 ml of a solution
containing 180.8 g of
magnesium chloride and
1786.7 g of calcium chloride
hexahydrate
Charge of chlorine 8 g per hour
Duration of the reaction 7 hours
Working temperature 85° C.
__________________________________________________________________________
KINETICS OF THE ATTACK
Composition
of the
fully dry
starting Composition of the solution after
product (g/l)
Element
(%) 30 m
1 h 2 h 3 h 4 h 5 h 6 h 7 h
__________________________________________________________________________
Zinc (Zn)
10.08 2.6 3.6 4.25
5.3 5.75
5.9 7 5.3
Lead (Pb)
6.88 0.02
0.013
0.45
0.80
1 1.15
1.50
1.85
Iron (Fe)
27 0.0095
0.0095
0.0095
0.0095
0.0095
0.0095
0.0095
0.0095
pH 5.8 5.2 4.1 3.8 3.7 3.6 3.4 3.3
__________________________________________________________________________
__________________________________________________________________________
BALANCE SHEET OF THE ATTACK
Yield of
Composition
COMPOSITION the attack
of the fully
of the
of the with res-
dry starting
mother-
washing
of the
pect to the
product
liquors
waters
residue
initial
Element (%) (g/l)
(g/l)
(%) product
__________________________________________________________________________
Zinc (Zn) 10.08 5.6 0.4 5.31
51.1
Lead (Pb) 6.88 1.9 0.082
5.50
25.2
Magnesium (Mg)
2.32 1.15
52.5
Calcium (Ca)
8.8 5.11
44.8
Iron (Fe) 27 0.01 0.004
20.38
0.06
Cadmium (Cd)
0.05
Manganese (Mn)
3.96
Silver (Ag)
88 ppm
Silica (SiO.sub.2)
3.68-3.76
Aluminium (Al.sub.2 O.sub.3)
0.91
__________________________________________________________________________
Volume of mother-liquors recovered
900 ml
Volume of washing waters recovered
600 ml
Weight of residual cake 95 g
__________________________________________________________________________
The mixtures of oxides treated in Examples XIII to XVI were the residues derived from a factory for the production of zinc situated in Crotone in Italy. The principal phases found in these residues are:
ZnFe.sub.2 O.sub.4 --CaSO.sub.4, 2H.sub.2 O--ZnS--PbSO.sub.4 --ZnSO.sub.4, H.sub.2 O and CaSO.sub.4 1/2H.sub.2 O
__________________________________________________________________________
Mixture to be treated 80 g of residue
Aqueous phase for the suspension
1000 ml of water
Charge of chlorine 8 g per hour
Duration of the reaction 6 hours
Working temperature 85° C.
__________________________________________________________________________
KINETICS OF THE ATTACK
Composition
of the
initial
Composition of the solution after
product
(g/l)
Element (%) 1 h 2 h 3 h 4 h 5 h 6 h
__________________________________________________________________________
Zinc (Zn)
13.5 3.5 3.7 3.7 4.2 4.3 4.6
Lead (Pb)
5.20 0.0058
0.00625
0.0074
0.008
0.0095
0.0106
Magnesium (Mg)
0.83 0.375
0.375
0.475
0.325
0.325
0.325
Calcium (Ca)
5.60 0.510
0.520
0.500
0.370
0.360
0.390
Iron (Fe)
15.6 0.083
0.104
0.115
0.225
0.275
0.350
pH 1.6 1.5 1.35
1.2 1.1 1.1
Chloride (Cl.sup.-)
-- 3.7 5 5.6 7.3 7.9 8.7
__________________________________________________________________________
__________________________________________________________________________
BALANCE SHEET OF THE ATTACK
Yield of
Composition
COMPOSITION the attack
of the fully
of the
of the with res-
dry starting
mother-
washing
of the
pect to the
product
liquors
waters
residue
initial
Element (%) (g/l)
(g/l)
(%) product
__________________________________________________________________________
Zinc (Zn)
13.5 5 0.5 8.97 41.5
Lead (Pb)
5.20 0.0105
0.0025
5.55 0.24
Magnesium (Mg)
0.83 0.425
0.047
0.13 80.4
Calcium (Ca)
5.60 0.520
0.440
3.64 20.9
Iron (Fe)
15.6 0.4 0.030
13.61
3.6
__________________________________________________________________________
Volume of mother-liquors recovered
900 ml
Volume of washing waters recovered
560 ml
Weight of residual cake 95 g
__________________________________________________________________________
__________________________________________________________________________
Mixture to be treated 80 g of residue
Aqueous phase fot the suspension
1000 ml of water
Charge of chlorine 8 g per hour
Duration of the reaction 6 hours
Working temperature 85° C.
__________________________________________________________________________
KINETICS OF THE ATTACK
Composition
of the
initial
Composition of the solution after
product
(g/l)
Element product
1 h 2 h 3 h 4 h 5 h 6 h
__________________________________________________________________________
Zinc (Zn)
11.3 0.9 1.2 1.3 1.3 1.8 1.8
Lead (Pb)
7.25 0.0045
0.0048
0.0056
0.0058
0.006
0.00625
Magnesium (Mg)
0.47 0.030
0.0325
0.034
0.035
0.036
0.037
Calcium (Ca)
5.68 0.420
0.440
0.440
0.390
0.440
0.450
Iron (Fe)
19.1 0.140
0.144
0.146
0.147
0.151
0.151
pH 1.75
1.70
1.65
1.60
1.55
1.50
Chloride (Cl.sup.-)
2.3 2.5 2.8 3 3.2 3.4
__________________________________________________________________________
__________________________________________________________________________
BALANCE SHEET OF THE ATTACK
Yield of
Composition
COMPOSITION the attack
of the fully
of the
of the with res-
dry starting
mother-
washing
of the
pect to the
product
liquors
waters
residue
initial
Element (%) (g/l)
(g/l)
(%) product
__________________________________________________________________________
Zinc (Zn)
11.3 1.7 0.16 9.52 18
Lead (Pb)
7.25 0.007
0.0025
6.95 0.2
Magnesium (Mg)
0.47 0.037
0.00004
0.41 8.6
Calcium (Ca)
5.68 0.590
0.360
21.1
Iron (Fe)
19.1 0.125
0.031
15.50
1.1
__________________________________________________________________________
Volume of mother-liquors recovered
890 ml
Volume of washing waters recovered
630 ml
Weight of residual cake 77 g
__________________________________________________________________________
The preceding description and examples allow those skilled in the art to appreciate the value and versatility of the process described above and to choose the correct operating conditions to solve their problems. They will moreover note the particular interest which there is in using this process to separate the nickel from cobalt and the iron contained in the basic carbonates of nickel and in the impure nickel oxides obtained from the roasting of mattes.
Claims (1)
1. A process for the selective dissolution of oxygenated compounds containing at least a nickel compound selected from the group consisting of nickel oxide, nickel carbonate and mixtures thereof, present in a mixture of oxygenated compounds containing said nickel compound and at least cobalt, copper and lead, comprising suspending the mixture of the oxygenated compounds in an aqueous phase, treating the resulting aqueous suspension at a pH exceeding about 1 and at a temperature of from about 60° to 100° C. with chlorine to selectively solubilize said nickel compound while said cobalt, copper and lead remain in an essentially insoluble residue, and separating the aqueous solution containing the dissolved said nickel compound from the insoluble residue.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7603266 | 1976-02-06 | ||
| FR7603266A FR2340376A1 (en) | 1976-02-06 | 1976-02-06 | HYDROMETALLURGIC PROCESS FOR THE SELECTIVE DISSOLUTION OF MIXTURES OF OXYGEN COMPOUNDS |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05950446 Continuation | 1978-10-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4435368A true US4435368A (en) | 1984-03-06 |
Family
ID=9168828
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/086,791 Expired - Lifetime US4435368A (en) | 1976-02-06 | 1979-10-22 | Hydrometallurgical process for selective dissolution of mixtures of oxy compounds |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4435368A (en) |
| JP (1) | JPS5296903A (en) |
| AU (1) | AU505079B2 (en) |
| BE (1) | BE850703A (en) |
| CA (1) | CA1096636A (en) |
| DE (1) | DE2705016A1 (en) |
| ES (1) | ES455649A1 (en) |
| FR (1) | FR2340376A1 (en) |
| GB (1) | GB1565752A (en) |
| IT (1) | IT1072388B (en) |
| NO (1) | NO770378L (en) |
| PH (1) | PH12063A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0244910A1 (en) * | 1986-05-06 | 1987-11-11 | Hoogovens Groep B.V. | Separation of non-ferrous metals from iron-containing powdery material |
| EP0248518A1 (en) * | 1986-04-24 | 1987-12-09 | Falconbridge Limited | Separation of nickel from copper in autoclave |
| US20040228783A1 (en) * | 2003-05-16 | 2004-11-18 | Jaguar Nickel Inc. | Process for the recovery of value metals from material containing base metal oxides |
| US20050118081A1 (en) * | 2003-09-30 | 2005-06-02 | Jaguar Nickel Inc. | Process for the recovery of value metals from base metal sulfide ores |
| US20070214912A1 (en) * | 2003-12-17 | 2007-09-20 | Fermag Inc. | Hydrometallurgical Separation Process Of Steel Mill Electric Arc Furnace (Eaf) Dust And The Pigments Obtained By The Process |
| US20080196619A1 (en) * | 2005-06-17 | 2008-08-21 | Ferrinov Inc. | Anti-Corrosion Pigments Coming Form Dust Of An Electric Arc Furnace And Containing Sacrificial Calcum |
| WO2012100293A1 (en) | 2011-01-25 | 2012-08-02 | The University Of Queensland | Improved method of ore processing |
| US20160355906A1 (en) * | 2011-01-25 | 2016-12-08 | The University Of Queensland | Method of ore processing |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5622603A (en) * | 1979-06-22 | 1981-03-03 | Nat Res Dev | Method of lixiviating chloride |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US350669A (en) | 1886-10-12 | Process of extracting metals from ores | ||
| US1736659A (en) | 1926-10-11 | 1929-11-19 | Lafayette M Hughes | Method of treating ores |
| US2971836A (en) | 1957-04-29 | 1961-02-14 | James D Hall | Separation of nickel and cobalt |
| US3647261A (en) | 1970-05-04 | 1972-03-07 | Dow Chemical Co | Process for solution mining of silver |
| US3880651A (en) | 1971-07-16 | 1975-04-29 | Paul Etienne Queneau | Chlorine leaching of non-ferrous metal values with ammoniacal solutions |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1456065A (en) * | 1971-03-18 | 1976-11-17 | Falconbridge Nickel Mines Ltd | Oxygen-acid leach process |
| US3880653A (en) * | 1971-03-18 | 1975-04-29 | Falconbridge Nickel Mines Ltd | Chlorine leach process |
| FR2152912A1 (en) * | 1971-09-10 | 1973-04-27 | Preussag Ag | Extraction of non-ferrous and noble metals from seawater - sludge - by treating with air and hydrogen sulphide |
| FR2262698B1 (en) * | 1974-02-28 | 1976-10-08 | Penarroya Miniere Metallurg |
-
1976
- 1976-02-06 FR FR7603266A patent/FR2340376A1/en active Granted
-
1977
- 1977-01-24 BE BE174341A patent/BE850703A/en not_active IP Right Cessation
- 1977-01-26 AU AU21659/77A patent/AU505079B2/en not_active Expired
- 1977-01-26 CA CA270,495A patent/CA1096636A/en not_active Expired
- 1977-02-02 GB GB4355/77A patent/GB1565752A/en not_active Expired
- 1977-02-04 NO NO770378A patent/NO770378L/en unknown
- 1977-02-04 JP JP1202777A patent/JPS5296903A/en active Pending
- 1977-02-04 ES ES455649A patent/ES455649A1/en not_active Expired
- 1977-02-04 IT IT1244977A patent/IT1072388B/en active
- 1977-02-07 DE DE19772705016 patent/DE2705016A1/en not_active Ceased
- 1977-02-07 PH PH19443A patent/PH12063A/en unknown
-
1979
- 1979-10-22 US US06/086,791 patent/US4435368A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US350669A (en) | 1886-10-12 | Process of extracting metals from ores | ||
| US1736659A (en) | 1926-10-11 | 1929-11-19 | Lafayette M Hughes | Method of treating ores |
| US2971836A (en) | 1957-04-29 | 1961-02-14 | James D Hall | Separation of nickel and cobalt |
| US3647261A (en) | 1970-05-04 | 1972-03-07 | Dow Chemical Co | Process for solution mining of silver |
| US3880651A (en) | 1971-07-16 | 1975-04-29 | Paul Etienne Queneau | Chlorine leaching of non-ferrous metal values with ammoniacal solutions |
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0248518A1 (en) * | 1986-04-24 | 1987-12-09 | Falconbridge Limited | Separation of nickel from copper in autoclave |
| EP0244910A1 (en) * | 1986-05-06 | 1987-11-11 | Hoogovens Groep B.V. | Separation of non-ferrous metals from iron-containing powdery material |
| US20040228783A1 (en) * | 2003-05-16 | 2004-11-18 | Jaguar Nickel Inc. | Process for the recovery of value metals from material containing base metal oxides |
| US7329396B2 (en) | 2003-05-16 | 2008-02-12 | Jaguar Nickel Inc. | Process for the recovery of value metals from material containing base metal oxides |
| US7736606B2 (en) | 2003-09-30 | 2010-06-15 | Jaguar Nickel Inc. | Process for the recovery of value metals from base metal sulfide ores |
| US20050118081A1 (en) * | 2003-09-30 | 2005-06-02 | Jaguar Nickel Inc. | Process for the recovery of value metals from base metal sulfide ores |
| US7968065B2 (en) | 2003-09-30 | 2011-06-28 | Jaguar Nickel Inc. | Process for the recovery of value metals from base metal sulfide ores |
| US20090013829A1 (en) * | 2003-09-30 | 2009-01-15 | Harris G Bryn | Process for the recovery of value metals from base metal sulfide ores |
| US20070214912A1 (en) * | 2003-12-17 | 2007-09-20 | Fermag Inc. | Hydrometallurgical Separation Process Of Steel Mill Electric Arc Furnace (Eaf) Dust And The Pigments Obtained By The Process |
| US20080196619A1 (en) * | 2005-06-17 | 2008-08-21 | Ferrinov Inc. | Anti-Corrosion Pigments Coming Form Dust Of An Electric Arc Furnace And Containing Sacrificial Calcum |
| US8016935B2 (en) | 2005-06-17 | 2011-09-13 | Ferrinov Inc. | Anti-corrosion pigments coming from dust of an electric arc furnace and containing sacrificial calcium |
| WO2012100293A1 (en) | 2011-01-25 | 2012-08-02 | The University Of Queensland | Improved method of ore processing |
| EP2668303A4 (en) * | 2011-01-25 | 2016-06-22 | Univ Queensland | IMPROVED PROCESS FOR PROCESSING ORE |
| US9447480B2 (en) | 2011-01-25 | 2016-09-20 | The University Of Queensland | Method of ore processing |
| US20160355906A1 (en) * | 2011-01-25 | 2016-12-08 | The University Of Queensland | Method of ore processing |
| KR101861885B1 (en) | 2011-01-25 | 2018-05-28 | 더 유니버서티 어브 퀸슬랜드 | Improved method of ore processing |
| US10662503B2 (en) | 2011-01-25 | 2020-05-26 | The University Of Queensland | Method of ore processing using mixture including acidic leach solution and oxidizing agent |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2340376A1 (en) | 1977-09-02 |
| FR2340376B1 (en) | 1979-07-20 |
| CA1096636A (en) | 1981-03-03 |
| PH12063A (en) | 1978-10-18 |
| ES455649A1 (en) | 1978-01-01 |
| NO770378L (en) | 1977-08-09 |
| IT1072388B (en) | 1985-04-10 |
| BE850703A (en) | 1977-07-25 |
| AU2165977A (en) | 1978-08-03 |
| DE2705016A1 (en) | 1977-08-18 |
| AU505079B2 (en) | 1979-11-08 |
| GB1565752A (en) | 1980-04-23 |
| JPS5296903A (en) | 1977-08-15 |
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